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ERGOTAMINE Safety Reports
Total ERGOTAMINE reports: 2.ERGOTAMINE FDA safety alerts: No.
Reported hospitalizations: 2.
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Health Professional from SPAIN reported ERGOTAMINE problem on May 23, 2007. Female patient, 48 years of age, was diagnosed with migraine and was treated with ERGOTAMINE. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, blood pressure increased, chest pain, coronary artery dissection, electrocardiogram st segment elevation, troponin t increased. ERGOTAMINE dosage: unknown. Patient was hospitalized. Patient recovered.
ERGOTAMINE problem was reported by a Health Professional from BELGIUM on July 11, 2003. Male patient, 68 years of age, was treated with ERGOTAMINE. After drug was administered, patient experienced the following problems/side effects: aortic dissection, aortic valve incompetence, cardiac murmur, chest pain, dyspnoea, hypertension, mitral valve prolapse, myocardial infarction, pulmonary hypertension. ERGOTAMINE dosage: unknown. During the same period patient was treated with AZATHIOPRINE, CYCLOSPORINE, PREDNISONE, IMMUNOSUPPRESSIVE AGENTS, AMLODIPINE, FUROSEMIDE, LISINOPRIL, CALCIUM ANTAGONIST. Patient was hospitalized. Patient recovered.